Canonical Allele Identifier: PA2826558235
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 230274
ClinVar RCV Id: RCV000219575 RCV000986022 RCV001294091 RCV002282052 RCV003475006 RCV002229212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Leu59Val
CA10579346
NM_001276503.2:c.175T>G